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Amyotrophie de Charcot-Marie-Tooth
Amyotrophie péronière
Atrophie de Charcot-Marie
Atrophie péronière
Diplégie faciale congénitale
Déjerine-Sottas
Hypertrophique de l'enfant
Maladie de Charcot-Marie
Maladie de Moebius
Migraine ophtalmoplégique
Ophtalmoplégie récidivante
Paralysie oculomotrice récidivante périodique
Syndrome d'hyper-réflectivité sinu-carotidienne
Syndrome de Charcot-Marie
Syndrome de Charcot-Marie-Tooth-Hoffmann
Syndrome de Charcot-Moebius
Syndrome de Charcot-Weiss-Baker
Syndrome de Moebius
Syndrome de Roussy-Lévy
Syndrome du sinus carotidien
Syndrome sinu-carotidien
Syndrome sinusal

Translation of "Syndrome de Charcot-Moebius " (French → English) :

migraine ophtalmoplégique | maladie de Moebius | syndrome de Charcot-Moebius | paralysie oculomotrice récidivante périodique | ophtalmoplégie récidivante

ophthalmoplegic migraine | Moebius disease | Moebius' disease | Möbius disease | Möbius syndrome | relapsing periodic oculomotor paralysis | relapsing ophthalmoplegia
médecine > sémiologie et pathologie | médecine > neurologie
médecine > sémiologie et pathologie | médecine > neurologie


maladie de Charcot-Marie | syndrome de Charcot-Marie | atrophie de Charcot-Marie | atrophie péronière | amyotrophie de Charcot-Marie-Tooth

Charcot-Marie-Tooth disease | peroneal muscular atrophy | progressive neuromuscular atrophy
médecine
médecine


syndrome de Charcot-Weiss-Baker | syndrome d'hyper-réflectivité sinu-carotidienne | syndrome du sinus carotidien | syndrome sinu-carotidien | syndrome sinusal

Charcot-Weiss-Baker syndrome
IATE - Health
IATE - Health


amyotrophie péronière | syndrome de Charcot-Marie-Tooth-Hoffmann

peroneal muscular atrophy | Charcot Marie-Tooth disease
médecine
médecine


diplégie faciale congénitale | syndrome de Moebius

infantile ocular muscle dystrophy | MOEBIUS Syndrom
IATE - Health
IATE - Health


syndrome de Moebius

A very rare congenital cranial dysinnervation disorder with characteristics of complete or incomplete facial paralysis in association with bilateral palsy of the abducens nerve causing impairment of ocular abduction. The syndrome also includes variou
SNOMEDCT-BE (disorder) / 766987006
SNOMEDCT-BE (disorder) / 766987006


syndrome de Moebius-neuropathie axonale-hypogonadisme hypogonadotrope

A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic.
SNOMEDCT-BE (disorder) / 724174003
SNOMEDCT-BE (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic. / 724174003


Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy

Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0


syndrome de maladie de Charcot-Marie-Tooth-surdité-déficience intellectuelle

A rare demyelinating hereditary motor and sensory neuropathy characterised by early-onset, slowly progressive, distal muscular weakness and atrophy with no sensory impairment, congenital sensorineural deafness and mild intellectual disability (with a
SNOMEDCT-BE (disorder) / 763136000
SNOMEDCT-BE (with a / 763136000




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Syndrome de Charcot-Moebius

Date index:2022-08-07 -

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